Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA10g17720 | A10 | 16905915 | G | A | missense_variant | MODERATE | c.920C>T|p.Pro307Leu |
S172 S217 |
2 | BAA10g17720 | A10 | 16906523 | C | T | splice_acceptor_variant&intron_variant | HIGH | c.608-1G>A| |
S125 |
3 | BAA10g17720 | A10 | 16907563 | C | T | stop_gained | HIGH | c.318G>A|p.Trp106* |
S46 |
4 | BAA10g17720 | A10 | 16908107 | C | T | synonymous_variant | LOW | c.72G>A|p.Lys24Lys |
S199 |
5 | BAA10g17720 | A10 | 16911481 | G | A | upstream_gene_variant | MODIFIER | c.-3303C>T| |
S151 S263 |
6 | BAA10g17720 | A10 | 16912199 | G | A | upstream_gene_variant | MODIFIER | c.-4021C>T| |
S178 |